Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment.

Synonyms: Vitreoretinal degeneration, Wagner type Wagner syndrome Dominant hyaloideoretinal dystrophy of Wagner VCAN-related vitreoretinopathy

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Term information

database cross reference
hasDbXref

UMLS:C0339540

ICD-10:H35.5

MedDRA:10063383

OMIM:143200

MeSH:C536075

UMLS:C1840452

notation

ORPHA:898